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Teen Diagnoses Her Own Disease In Science Class

18-year-old Jessica Terry suffered from stomach pain, diarrhea, vomiting and fever for eight years. She often missed school and her doctors were unable to figure out the cause of her sickness. Then one day in January someone was finally figured out what was wrong with Jessica. That person was her. While looking under a microscope at slides of her own intestinal tissue in her AP science class, Jessica noticed an area of inflamed tissue called a granuloma, which is an indication of Crohn's disease. "It's weird I had to solve my own medical problem," Terry told CNN affiliate KOMO in Seattle, Washington. "There were just no answers anywhere. ... I was always sick."

2 of 582 comments (clear)

  1. Hmm by El+Lobo · · Score: 5, Interesting

    Interesting: while reading about her symptoms, Crohn's Disease was the first think that came to my mind. And no, I'm not a doctor. So what kind of doctors were seeing her? Veterinary ones?

    --
    It's time to realise that Abble's products are the biggest abomination these days. Just say NO to the dumb iAbble way!!
  2. Some times you need to be your own advocate by hAckz0r · · Score: 5, Interesting
    My hat is off to this individual for being so resourceful at such an early age. I suffered from a parasitic disease for 37 years without any diagnosis, before buying all kinds of lab equipment and discovering the cause myself. The doctors never even tried to diagnose it, and some just labelled me as being a nut case, or something. I saw SO MANY doctors I have lost track, and not one of them really even tried to come up with an explanation, or send me for tests that might have even had a chance at diagnosing the actual problem. Not even so much as a guess. In short, they were incapable of 'thinking outside the box'.

    The answer was http://en.wikipedia.org/wiki/Schistosomiasis, which I contracted as a young child. It ruined my life, for sure. The trouble is, if you ask any doctor here in the US they will tell you it does not even exist here, only in west Africa and South America. I've never even been anywhere near there, or outside the country at the time at which I contracted it. If you have ever been labelled with IBS but have other symptoms as well then you might want to read the above wikipedia article.

    Because the doctors are not aware of the disease, they do not diagnose it.
    Because doctors do not diagnose it, they do not collect any statistics.
    Because the disease is statistically insignificant, the medical schools do not teach much, if any, about it.
    Therefore the doctors don't know about it.

    Anyone see a problem with this situation?

    What really hurts is that when it really started affecting my health my primary care physician at the time was an EXPERT in those diseases, and she just blew me off because it would bee too hard to think, or to send me for actual tests of some kind. You would never know her ineptitude by looking at her wall of certification she earned in medical school in west Africa. Of all doctors, including at least three infectious disease specialists, this one completely boggles my mind how she could have missed this diagnosis!

    After 37+ years of damage it took my buying my own 1600x stereo microscope mounted with a CCD camera to collect some indisputable evidence, one day to use it, one doctor visit to present my case, three days just to find a source in the US to fill the prescription, and only 24 hours to actually cure it. The damage was done, and nothing can ever give me back my health, or a normal life for that matter. The real kicker is my dog gets that exact same 'cure' every month, but it took me three days to find a supplier for a 'human' prescription for the exact same drug. All I can say is at least my dog has someone that actually cares about his health!